M81L (p.Met81Leu) variant of TNNC1 (P63316)
M81L (p.Met81Leu) in TNNC1 (P63316) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hypertrophic cardiomyopathy 13; Dilated cardiomyopathy 1Z; Cardiovascular phenot. The record also includes published literature and structural context.
M81L (p.Met81Leu) variant details
- p.Met81Leu
- rs2471444234
- ClinGen CA353167425
- ClinVar RCV002450387
- ClinVar RCV003775240
- Uncertain significance
- Hypertrophic cardiomyopathy 13; Dilated cardiomyopathy 1Z; Cardiovascular phenot
- Missense
- ClinVar: Uncertain significance (Hypertrophic cardiomyopathy 13; Dilated cardiomyopathy 1Z; Cardi)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of… (PMID 35802134)
- Cited in: Clinical utility gene card for: hypertrophic cardiomyopathy (type 1-14). (PMID 21267010)